A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1149198



Internal ID19195387
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:138718221..138718347hg38UCSC Ensembl
Outerchr7:138402966..138403092hg19UCSC Ensembl
Cytoband7q34
Allele length
AssemblyAllele length
hg38127
hg19127
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4002706
SamplesKWB1
Known GenesATP6V0A4
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceJohn_et_al_2014
Pubmed ID26484159
Accession Number(s)nsv1149198
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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